Aeruginosins, protease inhibitors from the cyanobacterium Microcystis aeruginosa

Aeruginosins, protease inhibitors from the cyanobacterium Microcystis aeruginosa
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DOI:
10.1016/s0040-4020(99)00621-3
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发表时间:
1999-09-03
期刊:
影响因子:
2.1
通讯作者:
Murakami, M
Murakami, M
中科院分区:
化学3区
文献类型:
--
作者:
Ishida, K;Okita, Y;Murakami, M

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从蓝细菌铜绿微囊藻中分离出五种新的蛋白酶抑制剂,分别与绿脓菌素298-A(5)、98-A(1)和98-B(2)相关。Aerodynosins 98-C(3)和101(4)在Hpla单位中不同于1。5例患者中的Aerodorosin 298-B(6)缺乏阿替诺单位。由于存在缩醛单元,在HPLC中以互变异构体的形式观察到Aerodorosins 89-A(7)和89-B(8)。根据降解产物的光谱数据和色谱分析确定结构3、4和6-8。1-8的绝对立体化学是通过光谱和化学研究相结合推导出来的。(C)1999爱思唯尔科技有限公司。保留所有权利。
Five new protease inhibitors, related to aeruginosins 298-A (5), 98-A (1) and 98-B (2), were isolated from the cyanobacterium Microcystis aeruginosa. Aeruginosins 98-C (3) and 101 (4) differed from 1 in the Hpla unit. Aeruginosin 298-B (6) lacked the argininol unit in 5. Aeruginosins 89-A (7) and 89-B (8) were observed as the tautomers in HPLC because of the presence of the argininal units. Structures 3, 4 and 6-8 were determined on the basis of spectral data and chromatographic analyses of degradation products. The absolute stereochemistry of 1-8 was deduced by a combination of spectral and chemical studies. (C) 1999 Elsevier Science Ltd. All rights reserved.